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ACT201 Injection in Healthy Participants and Participants With Chronic Hepatitis B (CHB)

perjantai 14. elokuuta 2026 päivittänyt: Xiamen Amoytop Biotech Co., Ltd.

A Single-Center, Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Phase I Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, Preliminary Efficacy, Drug Concentration-QTc Relationship, and Immunogenicity Profiles of Single and Multiple Doses of ACT201 Injection in Healthy Participants and Participants With Chronic Hepatitis B

This is a single-center, randomized, double-blind, placebo-controlled Phase I clinical trial consisting of two parts. Part 1 includes single ascending dose (SAD) and multiple ascending dose (MAD) cohorts conducted in healthy participants. Part 2 is a multiple ascending dose (MAD) trial enrolling HBeAg-negative chronic hepatitis B (CHB) participants with suppressed HBV DNA under stable nucleos(t)ide analog (NA) therapy.

Tutkimuksen yleiskatsaus

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

72

Vaihe

  • Vaihe 1

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskeluyhteys

Tutki yhteystietojen varmuuskopiointi

Opiskelupaikat

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Kiina
        • Rekrytointi
        • Huashan Hospital, Fudan University
        • Ottaa yhteyttä:
        • Ottaa yhteyttä:

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

  • Aikuinen
  • Vanhempi Aikuinen

Hyväksyy terveitä vapaaehtoisia

Joo

Kuvaus

Inclusion Criteria:

Part 1:

  • Participants fully understand the purpose, nature and methods of the trial as well as potential adverse events, voluntarily participate in this trial and provide written informed consent;
  • Aged between 18 and 55 years old (inclusive) at the time of informed consent, male or female;
  • Body mass index meets specified criteria;
  • Physical examination, vital signs, laboratory tests, electrocardiogram and imaging examinations at screening are normal or abnormalities are considered clinically insignificant;
  • Participants (including their partners) are willing to use effective contraceptive measures from screening through 6 months after the last administration of investigational product, with no plans for pregnancy, sperm donation or oocyte donation.

Part 2:

  • Participants fully understand the purpose, nature and methods of the trial as well as potential adverse events, voluntarily participate in this trial and provide written informed consent;
  • Aged between 18 and 65 years old (inclusive) at the time of informed consent, male or female;
  • Body mass index meets specified criteria;
  • HBsAg-positive or HBV DNA-positive for at least 6 months, or previous liver biopsy confirming chronic HBV infection;
  • Receiving stable nucleos(t)ide analogue (NA) therapy at screening, with no planned changes to NA regimen during the trial;
  • Serum ALT ≤ 2 × ULN at screening; HBeAg, HBV DNA and HBsAg levels meet protocol-specified criteria;
  • Participants (including their partners) are willing to use effective contraceptive measures from screening through 6 months after the last administration of investigational product, with no plans for pregnancy, sperm donation or oocyte donation.

Exclusion Criteria:

Part 1:

  • Known or suspected hypersensitivity to ACT201 or its excipients; or participants with allergic diathesis (multiple drug and food allergies judged clinically significant by the Investigator).
  • History of clinically significant diseases involving cardiovascular, hematologic and lymphatic, urinary, endocrine, immune, psychiatric, or nervous systems (e.g., epilepsy).
  • Vital signs or laboratory examinations at screening meet the exclusion cut-off values specified in the protocol.
  • Use of any prescription drugs, over-the-counter medications, vitamin products or herbal medicines within 2 weeks prior to the first dose (topical medications with local effects are excluded).
  • Positive HBsAg, hepatitis B core antibody, hepatitis C antibody, human immunodeficiency virus antibody, or Treponema pallidum antibody at screening.
  • QTcF interval (QT corrected by Fridericia's formula) > 450 ms at screening.
  • Daily cigarette consumption exceeding 5 cigarettes within 3 months before screening.
  • History of drug abuse or illicit drug use within 1 year before screening, or positive urine drug screen at screening.
  • History of alcohol abuse within 6 months before screening (14 alcohol units per week: 1 unit = 285 mL beer with ~3.5% alcohol, or 25 mL spirits with ~40% alcohol, or 100 mL wine with ~10% alcohol), or positive breath alcohol test at screening.
  • Vaccination administered within 1 month before screening, or planned vaccination during the trial period.
  • Blood loss or blood donation ≥ 400 mL within 3 months before screening (menstrual bleeding in female participants excluded), or planned blood donation during the trial period.
  • Female participants who are breastfeeding or have a positive serum pregnancy test at screening.
  • Participation in any clinical trial with an investigational medicinal product/investigational device within 3 months before screening or within 5 half-lives (whichever is longer).
  • Any other condition deemed unsuitable for trial participation by the Investigator.

Part 2:

  • Major trauma or major surgery within 3 months before screening; or planned surgery during the trial period that may impair trial compliance or safety assessment as assessed by the Investigator.
  • Uncontrolled and clinically significant abnormalities other than chronic HBV infection, such as acute cerebrovascular disease, severe or unstable cardiac disease, uncontrolled diabetes, uncontrolled hypertension, uncontrolled dyslipidemia, etc.
  • History of other clinically significant liver diseases.
  • History of liver cirrhosis or progressive liver fibrosis; or liver stiffness measurement (LSM) ≥ 8.5 kPa at screening.
  • Alpha-fetoprotein > 50 ng/mL, or imaging suggestive of possible malignant hepatic lesions.
  • Past or current manifestations of hepatic decompensation.
  • History of extrahepatic diseases potentially related to HBV immune status.
  • History of vasculitis; or signs/symptoms suggestive of underlying vasculitis; or past/current other diseases potentially associated with vasculitic disorders.
  • Active infection requiring systemic antiviral or antibacterial treatment at screening, excluding HBV infection.
  • History of malignant tumors within 5 years before screening, except for specific curable cancers resected surgically.
  • Prior solid organ or bone marrow transplantation.
  • Use of systemic immunosuppressants within 3 months before the first dose of investigational product [short-term (≤7 days) glucocorticoids for prophylaxis or treatment of non-autoimmune diseases excluded]; use of immunomodulators or cytotoxic agents within 6 months before the first dose of investigational product.
  • Receipt of any oligonucleotide or small interfering RNA (siRNA) therapy within 12 months before the first dose of investigational product.
  • Coexisting indication for anticoagulant therapy or anticipated requirement for anticoagulation during the trial.
  • Any of the following laboratory results at screening, or other clinically significant abnormalities rendering the participant unsuitable for trial participation:

Platelet count < 125 × 10^9/L Absolute neutrophil count < 1.5 × 10^9/L Hemoglobin < 100 g/L Total bilirubin > 1.25 × ULN Serum albumin < 35 g/L Estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73 m^2 (calculated using the CKD-EPI formula) Prothrombin time international normalized ratio (INR) > 1.25 Positive hepatitis C antibody, human immunodeficiency virus antibody, or Treponema pallidum antibody

  • QTcF interval (QT corrected by Fridericia's formula) > 450 ms at screening, or other clinically significant electrocardiogram abnormalities identified at screening.
  • Known or suspected hypersensitivity to ACT201 or its excipients; or participants with allergic diathesis (multiple drug and food allergies judged clinically significant by the Investigator).
  • Daily cigarette consumption exceeding 5 cigarettes within 3 months before screening.
  • History of drug abuse or illicit drug use within 1 year before screening, or positive urine drug screen at screening.
  • History of alcohol abuse within 6 months before screening, or positive breath alcohol test at screening.
  • Vaccination administered within 1 month before screening, or planned vaccination during the trial period.
  • Blood loss or blood donation ≥ 400 mL within 3 months before screening (menstrual bleeding in female participants excluded), or planned blood donation during the trial period.
  • Female participants who are breastfeeding or have a positive serum pregnancy test at screening.
  • Participation in any clinical trial with an investigational medicinal product/investigational device within 3 months before screening or within 5 half-lives (whichever is longer).
  • Any other condition deemed unsuitable for trial participation by the Investigator.

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Hoito
  • Jako: Satunnaistettu
  • Inventiomalli: Peräkkäinen tehtävä
  • Naamiointi: Kaksinkertainen

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: ACT201 Injection group

Part 1 SAD (Single Ascending Dose): Single-dose subcutaneous injection per assigned dose group.

Part 1 MAD (Multiple Ascending Dose) and Part 2: Subcutaneous injection per assigned dose group; treatment duration shall follow the study protocol.

Placebo Comparator: ACT201 Injection Placebo

Part 1 SAD (Single Ascending Dose): Single-dose subcutaneous injection administered per assigned dose group.

Part 1 MAD (Multiple Ascending Dose) and Part 2: Subcutaneous injection administered per assigned dose group; the treatment duration shall comply with the study protocol.

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Safety: number of participants with adverse event (AE), serious adverse events (SAE) and clinically significant examination results.
Aikaikkuna: throughout the full study period,an average of 4 months
Assessments include vital signs, physical examinations, laboratory tests, and 12-lead electrocardiograms (ECGs).
throughout the full study period,an average of 4 months

Toissijaiset tulostoimenpiteet

Tulosmittaus
Aikaikkuna
Plasma drug concentrations in healthy participants and participants withCHB
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Area Under the Concentration-Time Curve from time zero to the last measurable concentration(AUC₀-ₜ)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Area Under the Concentration-Time Curve from time zero to infinity(AUC₀-∞)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Apparent Volume of Distribution(Vd/F)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
First-order Elimination Rate Constant(Kel)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Elimination Half-life(t₁/₂)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Mean Residence Time(MRT)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Apparent Clearance(CL/F)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Minimum Plasma Concentration at Steady State(Cₘᵢₙ,ₛₛ)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Maximum Plasma Concentration at Steady State(Cₘₐₓ,ₛₛ)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Average Plasma Concentration at Steady State(Cₐᵥ,ₛₛ)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Area Under the Concentration-Time Curve over one dosing interval at steady state(AUC₀-τ)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Degree of Fluctuation (DF)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Accumulation Factor (Rac)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Urinary Concentration
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Cumulative Amount Excreted in Urine
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Cumulative Percentage of Dose Excreted in Urine
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Renal Clearance(CL)
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
HBsAg and HBsAb levels and changes from baseline among participants with CHB
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
HBsAg seroclearance rate among participants with CHB
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
HBsAg seroconversion rate among participants with CHB
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Placebo-corrected baseline-adjusted ΔQTc (ΔΔQTc) among healthy participants
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Anti-drug antibody (ADA) positive rate among healthy participants and participants with CHB
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Antibody titers among healthy participants and participants with CHB
Aikaikkuna: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Yhteistyökumppanit

Tutkijat

  • Päätutkija: Jing Zhang, Ph.D., Huashan Hospital
  • Päätutkija: Wenhong Zhang, Ph.D., Huashan Hospital

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus (Todellinen)

Torstai 6. elokuuta 2026

Ensisijainen valmistuminen (Arvioitu)

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Opintojen valmistuminen (Arvioitu)

Torstai 1. huhtikuuta 2027

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Maanantai 20. heinäkuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Keskiviikko 29. heinäkuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Maanantai 3. elokuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Maanantai 17. elokuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Perjantai 14. elokuuta 2026

Viimeksi vahvistettu

Lauantai 1. elokuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Muut tutkimustunnusnumerot

  • ACT201-4-1-001

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